Results 151 to 157 of about 1,391 (157)

Carrier frequency of the 35delG and A1555G deafness mutations in the Argentinean population

International Journal of Pediatric Otorhinolaryngology, 2007
Luis Pablo Gravina
exaly  

The frequency of the homozygote 35delG mutation in the connexin 26 gene in North African with non-syndromic hearing loss: A meta-analysis study

Meta Gene, 2021
exaly  

Prevalence of the c.35delG and p.W24X mutations in the GJB2 gene in patients with nonsyndromic hearing loss from North-West Romania

International Journal of Pediatric Otorhinolaryngology, 2010
Adrian Pavel Trifa, Camelia Al-Khzouz
exaly  

Connexin 26 35delG does not represent a mutational hotspot

Human Genetics, 2003
Alessandra Murgia, Emanuela Leonardi, Sarah L Lebeis   +2 more
exaly  

Phenotypic variability of patients homozygous for the GJB2 mutation 35delG cannot be explained by the influence of one major modifier gene

European Journal of Human Genetics, 2008
Guy Van Camp, Klemens Frei, Alessandra Murgia   +2 more
exaly  

A simple PCR test to detect the common 35delG mutation in the connexin 26 gene

Molecular Diagnosis and Therapy, 2000
exaly  

Frequency of the 35delG mutation in the connexin 26 gene in Turkish hearing-impaired patients

Clinical Genetics, 2001
exaly